Canonical Allele Identifier: PA163627
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140810
ClinVar RCV Id: RCV000128997 RCV000228319 RCV000235651 RCV001269353 RCV000759122 RCV003333736 RCV003997470 RCV004532540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro259Ser
CA022230
NM_000251.3:c.775C>T